Clinical Trial Assistant
Core
Provide operational support to coordinate the conduct and management of clinical studies, ensuring compliance with standard operating procedures, Good Clinical Practices (GCP), and applicable regulations.
Role type
Clinical Trial Assistant
Builds
Clinical study execution and regulatory compliance
Domain
Medical device clinical trials
Deliverable
client delivery
Required skills
Clinical trial coordination, regulatory compliance knowledge, document management, budget tracking, supply chain logistics, meeting coordination
Preferred skills
Medical device clinical trials experience, regulatory support, clinical project coordination, basic medical terminology, Good Clinical Practice knowledge
Technologies
MS Office, Adobe, video and web conferencing solutions
Responsibilities
Coordinate and manage ordering, shipping, labeling, and tracking of study supplies; Establish and maintain electronic study files and trial master files; Facilitate approval and signature routing for clinical study documents; Support study budget tracking and payments; Prepare and ship site and patient binders; Collaborate with Clinical Study Managers to develop informational materials; Provide administrative support for study and investigator meetings
Seniority
Mid-level, hands-on support
